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Dominant-negative diabetes insipidus and other endocrinopathies
Familial neurohypophyseal diabetes insipidus (FNDI) in humans is an autosomal dominant disorder caused by a variety of mutations in the arginine vasopressin (AVP) precursor. A new report demonstrates how heterozygosity for an AVP mutation causes FNDI (see the related article beginning on page 1697)....
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| Pubblicato in: | J Clin Invest |
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| Autore principale: | |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Clinical Investigation
2003
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC281655/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14660740/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI20441 |
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